Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Bragagni A."'
Publikováno v:
Università degli studi di Firenze-IRIS
The objective of this study was the development of a niosomal formulation for improving skin permeation and penetration of 5-aminolevulinic acid (ALA) in the treatment of skin malignancies by photodynamic therapy (PDT). Different niosomal dispersions
Autor:
Marco Bragagni, Paola Mura, Maria Esther Gil-Alegre, Carla Ghelardini, Marzia Cirri, Lorenzo Di Cesare Mannelli
Publikováno v:
International journal of pharmaceutics. 547(1-2)
A delivery system based on poly(lactic-co-glycolic acid) polymer (PLGA) microparticles has been developed for parenteral administration of the local anesthetic prilocaine in its free base form. Both drug-free and drug-loaded microparticles, prepared
Autor:
Bragagni, Marco1 (AUTHOR), Mennini, Natascia1 (AUTHOR), Maestrelli, Francesca1 (AUTHOR), Cirri, Marzia1 (AUTHOR), Mura, Paola1 (AUTHOR) paola.mura@unifi.it
Publikováno v:
Drug Delivery. Sep/Oct2012, Vol. 19 Issue 7, p354-361. 8p.
Publikováno v:
Drug Delivery. 19:354-361
Topical administration of celecoxib proved to be an effective mean of preventing skin cancer development and improving anticancer drugs effectiveness in skin tumors treatment. The aim of this study was the development of an effective topical formulat
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 80:46-53
A new delivery system based on drug cyclodextrin (Cd) complexation and loading into nanostructured lipid carriers (NLC) has been developed to improve ketoprofen therapeutic efficacy. The proposed strategy exploits both the solubilizing and stabilizin
Publikováno v:
Journal of Microencapsulation. 27:479-486
A combined approach based on drug cyclodextrin (CD) complexation and loading into PLGA nanoparticles (NP) has been developed to improve oxaprozin therapeutic efficiency. This strategy exploits the solubilizing and stabilizing properties of CDs and th
Publikováno v:
International journal of pharmaceutics. 475(1-2)
Transdermal administration of clonazepam, a poorly water-soluble benzodiazepine, is an interesting strategy for overcoming the drawbacks of its oral administration. With this aim, two nano-carrier formulations, based on ultra-deformable liposomes and
Autor:
Sandra Furlanetto, Carla Ghelardini, Paola Mura, Marco Bragagni, Serena Orlandini, Natascia Mennini
Publikováno v:
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V. 87(1)
A niosomal formulation, functionalized with N-palmitoylglucosamine, was developed as potential brain targeted delivery system of dynorphin-B. In fact, this endogenous neuropeptide, selective agonist of k opioid receptors, is endowed with relevant pha
Autor:
Sandra Furlanetto, Lorenzo Di Cesare Mannelli, Carla Ghelardini, Natascia Mennini, Paola Mura, Marco Bragagni
Publikováno v:
Drug development and industrial pharmacy. 40(11)
Celecoxib is an anti-inflammatory drug, specific inhibitor of COX-2, classified as a BCS class II compound due to its very low aqueous solubility (3 μg/mL) and good permeability.An innovative micellar formulation of celecoxib has been developed to i
Autor:
Cristina Muñoz-San Martín, Paola Mura, Maria Esther Gil-Alegre, Marco Bragagni, Dolores Hernán Pérez de la Ossa, Cristina Beneitez
The use of injectable local anaesthetics for the treatment of severe postoperative pain is limited by the short duration of the painkilling effect. Pre-formulation studies were carried out for the development of an injectable microparticle formulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85752fd06985370391e32e5d5d229a4
http://hdl.handle.net/2158/794880
http://hdl.handle.net/2158/794880